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01 1Alginic Acid Alumina; Hydrated Sodium Bicarbonate

02 2Allopurinol

03 1Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate

04 2Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide

05 1Apricot

06 1Aprotinin, Bovint

07 1Cetirizine Dihydrochloride

08 2DESMOPRESSIN ACETATE

09 3Desloratadine

10 3Dexibuprofen

11 1Docetaxel (Vattenfri)

12 1Doxycycline Hyclate

13 1Doxycycline Monohydrate

14 2Gimeracil; Oteracil Potassium; Tegafur

15 1Glucosamine Sulfate Potassium Chloride

16 1Loperamide Hydrochloride

17 1Loperamide Hydrochloride; Simethicone

18 8METHOTREXATE

19 5METHOTREXATE (METHOTREXATE SODIUM)

20 75Metadonhydroklorid

21 64Methotrexate

22 8Methotrexate Disodium

23 8Metotreksat

24 1Misoprostol

25 2My Firstborn

26 5Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

27 2Paracetamol

28 2Ranitidine Hydrochloride

29 1Sodium Hyaluronate

30 1Sodium Picosulfate (Monohydrate)

31 2Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate

32 3Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate; Calcium carbonate

33 4Tegafur; Gimeracil; Oteracilmonokalium

34 2Tegafur; Gimeracil; Oteracil

35 4Tegafur; Gimeracil; Oteracyl Potassium

36 1Terbinafinhydrochloride

37 3Xylometazoline Hydrochloride

38 4Ziprasidone Hydrochloride (Anhydrous)

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PharmaCompass

01

Brand Name : Gaviscon

IMCAS World Congress
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Brand Name : Gaviscon

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Nordic Drugs

Dosage Form : Chewable Tablet

Brand Name : Gaviscon

Dosage Strength :

Packaging :

Approval Date : 30/08/1974

Application Number : 19740830000013

Regulatory Info : Approved

Registration Country : Sweden

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02

Brand Name : Allopurinol Nordic D...

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Brand Name : Allopurinol Nordic D...

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Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Brand Name : Allopurinol Nordic Drugs

Dosage Strength : 100mg

Packaging :

Approval Date : 25/01/1991

Application Number : 19910125000015

Regulatory Info : Approved

Registration Country : Sweden

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03

Brand Name : Allopurinol Nordic D...

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Brand Name : Allopurinol Nordic D...

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Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Brand Name : Allopurinol Nordic Drugs

Dosage Strength : 300mg

Packaging :

Approval Date : 25/01/1991

Application Number : 19910125000022

Regulatory Info : Approved

Registration Country : Sweden

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04

Brand Name : Gaviscon

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Brand Name : Gaviscon

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Not Confirmed

Nordic Drugs

Dosage Form : Oral Suspension

Brand Name : Gaviscon

Dosage Strength :

Packaging :

Approval Date : 05/02/1982

Application Number : 19820205000135

Regulatory Info : Approved

Registration Country : Sweden

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05

Brand Name : Amyloferm

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Brand Name : Amyloferm

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Nordic Drugs

Dosage Form : Tablet

Brand Name : Amyloferm

Dosage Strength : 5mg;50mg

Packaging :

Approval Date : 04/05/1990

Application Number : 19900504000149

Regulatory Info : Approved

Registration Country : Sweden

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06

Brand Name : Amyloferm Mite

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Brand Name : Amyloferm Mite

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Nordic Drugs

Dosage Form : Tablet

Brand Name : Amyloferm Mite

Dosage Strength : 2.5mg;25mg

Packaging :

Approval Date : 04/05/1990

Application Number : 19900504000156

Regulatory Info : Approved

Registration Country : Sweden

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07

Brand Name : Trasylol

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Brand Name : Trasylol

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Nordic Pharma

Dosage Form : Solution For Injection/I...

Brand Name : Trasylol

Dosage Strength :

Packaging :

Approval Date : 16/03/1977

Application Number : 38837

Regulatory Info : Allowed

Registration Country : Switzerland

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08

Brand Name : Trasylol

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Brand Name : Trasylol

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Nordic Pharma

Dosage Form : Solution For Injection/I...

Brand Name : Trasylol

Dosage Strength : 10000KIE/ml

Packaging :

Approval Date : 13/12/1967

Application Number : 19671213000033

Regulatory Info : Approved

Registration Country : Sweden

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09

Brand Name : Acura

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Brand Name : Acura

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Nordic Drugs

Dosage Form : Film Coated Tablet

Brand Name : Acura

Dosage Strength : 10mg

Packaging :

Approval Date : 19/04/2002

Application Number : 20020419000112

Regulatory Info : Deregistered

Registration Country : Sweden

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10

Brand Name : Desloraphar

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Brand Name : Desloraphar

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Disphar International

Dosage Form : Film Coated Tablet

Brand Name : Desloraphar

Dosage Strength : 5mg

Packaging :

Approval Date : 13/09/2012

Application Number : 20110121000033

Regulatory Info : Deregistered

Registration Country : Sweden

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